EP2182091A1 - Liquide de traitement de film isolant pour une tôle d'acier électromagnétique à grains orientés, et procédé pour produire une tôle d'acier électromagnétique à grains orientés avec un film isolant - Google Patents

Liquide de traitement de film isolant pour une tôle d'acier électromagnétique à grains orientés, et procédé pour produire une tôle d'acier électromagnétique à grains orientés avec un film isolant Download PDF

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Publication number
EP2182091A1
EP2182091A1 EP08792758A EP08792758A EP2182091A1 EP 2182091 A1 EP2182091 A1 EP 2182091A1 EP 08792758 A EP08792758 A EP 08792758A EP 08792758 A EP08792758 A EP 08792758A EP 2182091 A1 EP2182091 A1 EP 2182091A1
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Prior art keywords
grain oriented
insulation coating
mol
oriented electrical
electrical steel
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EP08792758A
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German (de)
English (en)
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EP2182091A4 (fr
EP2182091B1 (fr
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Minoru Takashima
Mineo Muraki
Makoto Watanabe
Tomofumi Shigekuni
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JFE Steel Corp
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JFE Steel Corp
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    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D6/00—Heat treatment of ferrous alloys
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/12—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties
    • C21D8/1216—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties the working step(s) being of interest
    • C21D8/1233—Cold rolling
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/12—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties
    • C21D8/1277—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties involving a particular surface treatment
    • C21D8/1283—Application of a separating or insulating coating
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/12—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties
    • C21D8/1277—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties involving a particular surface treatment
    • C21D8/1288—Application of a tension-inducing coating
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
    • C21D9/46—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for sheet metals
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22C—ALLOYS
    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22C—ALLOYS
    • C22C38/00—Ferrous alloys, e.g. steel alloys
    • C22C38/60—Ferrous alloys, e.g. steel alloys containing lead, selenium, tellurium, or antimony, or more than 0.04% by weight of sulfur
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
    • C23C22/05—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
    • C23C22/06—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
    • C23C22/07—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing phosphates
    • C23C22/08—Orthophosphates
    • C23C22/18—Orthophosphates containing manganese cations
    • C23C22/182—Orthophosphates containing manganese cations containing also zinc cations
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
    • C23C22/05—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
    • C23C22/06—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
    • C23C22/07—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing phosphates
    • C23C22/08—Orthophosphates
    • C23C22/18—Orthophosphates containing manganese cations
    • C23C22/188—Orthophosphates containing manganese cations containing also magnesium cations
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
    • C23C22/05—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
    • C23C22/06—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
    • C23C22/07—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing phosphates
    • C23C22/08—Orthophosphates
    • C23C22/20—Orthophosphates containing aluminium cations
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
    • C23C22/05—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
    • C23C22/06—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
    • C23C22/07—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing phosphates
    • C23C22/08—Orthophosphates
    • C23C22/22—Orthophosphates containing alkaline earth metal cations
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
    • C23C22/73—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals characterised by the process
    • C23C22/74—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals characterised by the process for obtaining burned-in conversion coatings
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
    • H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
    • H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
    • H01F1/12—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials
    • H01F1/14—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials metals or alloys
    • H01F1/16—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials metals or alloys in the form of sheets
    • H01F1/18—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials metals or alloys in the form of sheets with insulating coating
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F27/00—Details of transformers or inductances, in general
    • H01F27/23—Corrosion protection
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/12—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties
    • C21D8/1216—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties the working step(s) being of interest
    • C21D8/1222—Hot rolling
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/12—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties
    • C21D8/1244—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties the heat treatment(s) being of interest
    • C21D8/1272—Final recrystallisation annealing
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
    • H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
    • H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
    • H01F1/12—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials
    • H01F1/14—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials metals or alloys
    • H01F1/147—Alloys characterised by their composition
    • H01F1/14766—Fe-Si based alloys
    • H01F1/14791—Fe-Si-Al based alloys, e.g. Sendust

Definitions

  • the present invention relates to a treatment solution for insulation coating for grain oriented electrical steel sheet for use in the production of a grain oriented electrical steel sheet excellent in tension induced by a coating, moisture-absorption resistance, rust resistance, and lamination factor.
  • the present invention also relates to a method for producing a grain oriented electrical steel sheet having an insulation coating using the treatment solution for insulation coating for grain oriented electrical steel sheet.
  • the noise from power transformers poses problems as environmental pollution.
  • the noise of power transformers is mainly caused by magnetostriction of a grain oriented electrical steel sheet used as an iron core material of transformers.
  • magnetostriction of the grain oriented electrical steel sheet In order to reduce the noise of transformers, it is required to reduce the magnetostriction of the grain oriented electrical steel sheet.
  • An industrially advantageous solution is to cover the grain oriented electrical steel sheet with an insulation coating.
  • tension induced by a coating As properties required for insulation coatings for grain oriented electrical steel sheets, tension induced by a coating, moisture-absorption resistance, rust resistance, and lamination factor are mentioned. Among the properties, securing the tension induced by a coating is important for the reduction in the magnetostriction.
  • the tension induced by a coating refers to tension given to grain oriented electrical steel sheets by the formation of insulation coatings.
  • the coatings of grain oriented electrical steel sheets generally contain a ceramic forsterite coating formed by secondary recrystallization annealing and a phosphate-based insulation coating provided thereon.
  • a method for forming the insulation coating techniques disclosed in Japanese Unexamined Patent Application Publication Nos. 48-39338 (Patent Document 1) and 50-79442 (Patent Document 2) are known. In these techniques, a treatment solution for insulation coating containing colloidal silica, phosphates, and chromium compounds (e.g., one or two or more members selected from chromic anhydrides, chromates, and dichromates) is applied to a steel sheet, and then the steel sheet is baked.
  • colloidal silica, phosphates, and chromium compounds e.g., one or two or more members selected from chromic anhydrides, chromates, and dichromates
  • the insulation coatings formed by these methods have effects of improving the magnetostriction properties by giving tensile stress to grain oriented electrical steel sheets.
  • the treatment solutions for insulation coating contain chromium compounds, such as chromic anhydrides, chromates, or dichromates, as components for maintaining favorable moisture-absorption resistance of the insulation coating, resulting in the fact that the treatment solutions for insulation coating contain hexachromium derived from the chromium compounds.
  • Patent Document 2 also discloses a technique of adding no chromium compounds. However, the technique is extremely disadvantageous from the viewpoint of moisture-absorption resistance.
  • the hexachromium contained in the treatment solution for insulation coating is reduced into trivalent chromium by baking to be detoxicated.
  • Patent Document 3 discloses a treatment solution for insulation coating containing colloidal silica, aluminum phosphate, and boric acid, and further containing one or two or more members selected from sulfates of Mg, Al, Fe, Co, Ni, and Zn. Moreover, Japanese Examined Patent Application Publication No.
  • Patent Document 4 also discloses a treatment solution for insulation coating containing colloidal silica and magnesium phosphate and further containing one or two or more members selected from sulfates of Mg, Al, Mn, and Zn.
  • the use of the treatment solutions for insulation coating of Patent Documents 3 and 4 has caused problems in terms of tension induced by a coating and moisture-absorption resistance in a request to coating properties in recent years.
  • Patent Document 5 discloses a treatment solution for insulation coating in which a compound containing a permanganate ion has been added to an aqueous solution of magnesium phosphate and/or aluminum phosphate.
  • the treatment solution for insulation coating of Patent Document 5 does not contain colloidal silica, and thus is disadvantageous from the viewpoint of the tension induced by a coating.
  • the present invention has been developed in view of the above-described present circumstances, and aims to achieve each following item.
  • the present inventors apply a treatment solution for insulation coating containing various water-soluble metal salts in addition to phosphate and colloidal silica to a grain oriented electrical steel sheet after subjected to secondary recrystallization annealing, and then baking the grain oriented electrical steel sheet. Then, the properties of the obtained coating have been examined.
  • an insulation coating having desired properties can be obtained by adding permanganates of divalent metals, such as Mg, Sr, Zn, Ba, and Ca.
  • the present invention has been accomplished based on the above-described findings.
  • the gist and the composition of the present invention are as follows.
  • the treatment solution for insulation coating is chromium-free and, particularly preferably, the treatment solution for insulation coating does not substantially contain Cr.
  • the treatment solution is preferably a water-based solution.
  • the rolling it is preferable to achieve the final sheet thickness by performing cold rolling once, or twice or more including intermediate annealing, after hot rolling or further performing normalizing annealing. Furthermore, it is preferable to apply an annealing separator containing MgO as a primary component after the primary recrystallization annealing, and then perform the secondary recrystallization annealing.
  • treatment solutions for insulation coating were prepared by mixing the following compounds:
  • the treatment solutions for insulation coating were applied to a grain oriented electrical steel sheet (sheet thickness: 0.22 mm) having a forsterite coating after subjected to the secondary recrystallization annealing, and baked at 800°C for 60 seconds, thereby forming an insulation coating so that the thickness per one side is 2 ⁇ m.
  • the grain oriented electrical steel sheet thus obtained was evaluated for the tension induced by a coating, moisture-absorption resistance, rust resistance, and lamination factor by methods described below.
  • Test pieces having a width of 30 mm and a length of 280 mm were extracted by shearing from the grain oriented electrical steel sheet having an insulation coating such a manner that the lengthwise direction was set to the rolling direction. Subsequently, the insulation coating on one of the both faces is removed. The dimension of the amount of curvature deformation of one end of the test pieces was measured while fixing one end having a length of 30 mm in the lengthwise direction of the steel sheet, and the tension induced by a coating ⁇ was calculated from Equation (1). In order to eliminate the effects of the self weight of the steel sheet, the amount of curvature deformation was measured in such a manner that the lengthwise direction of the steel sheet was set to the horizontal direction and the width direction was set to the vertical direction, respectively.
  • ⁇ MPa 1.2152 ⁇ 10 5 MPa ⁇ Sheet thickness mm ⁇ Deformation mm / 250 mm / 250 mm
  • test pieces 50 mm ⁇ 50 mm
  • the amount of P eluted from the coating surface was quantitatively analyzed, and the average value was determined to be used as the index of the moisture-absorption resistance.
  • the steel sheet having an insulation coating was held in the air having a temperature of 50°C and a dew point of 50°C for 50 hours, and then the steel sheet surface was visually observed. Then, the steel sheet free from the formation of rust was defined as (OK) and the steel sheet suffering from the formation of rust was defined as (NG).
  • the area ratio of the rust is approximately lower than 5% when evaluated as (OK) and is approximately 5% or more when evaluated as (NG).
  • the lamination factor was evaluated by a method based on JIS C 2550.
  • Fig. 1 shows effects of the addition amount of magnesium permanganate ⁇ hexahydrate (Axis of abscissa: Addition amount to PO 4 :1 mol) to a treatment solution for insulation coating on the amount of elution of P, i.e., moisture-absorption resistance, of an insulation coating (Axis of ordinates: per 150 cm 2 , Unit: ⁇ g).
  • Fig. 2 shows effects of the addition amount of magnesium permanganate ⁇ hexahydrate (Axis of abscissa) on the tension induced by a coating of an insulation coating (Axis of ordinates, Unit: MPa).
  • the addition amount of the magnesium permanganate ⁇ hexahydrate in Figs. 1 and 2 is the number of moles in terms of Mg.
  • the rust resistance and the lamination factor were excellent when the addition amount of magnesium permanganate ⁇ hexahydrate was in the range of 0.02 to 2.5 mol in terms of Mg.
  • the treatment solution for insulation coating of the present invention is preferably a water-based solution. More specifically, the treatment solution for insulation coating of the invention contains at least one member selected from phosphates of Mg, Ca, Ba, Sr, Zn, Al, and Mn, colloidal silica, and at least one member selected from permanganates of Mg, Sr, Zn, Ba, and Ca, in which water is preferably used as a solvent.
  • the phosphates it is required to select one or two or more members from phosphates of Mg, Ca, Ba, Sr, Zn, Al, and Mn and incorporate the same in the treatment solution for insulation coating. This is because, in the case of phosphates other than the phosphates mentioned above, a coating having favorable moisture-absorption resistance is not obtained when adding no chromium compounds (e.g., chromates).
  • Mg(H 2 PO 4 ) 2 , Ca(H 2 PO 4 ) 2 , Ba(H 2 PO 4 ) 2 , Sr(H 2 PO 4 ) 2 , Zn(H 2 PO 4 ) 2 , Al(H 2 PO 4 ) 3 , and Mn(H 2 PO 4 ) 2 which are primary phosphates of Mg, Ca, Ba, Sr, Zn, Al, and Mn easily dissolve in water, and thus can be preferably used for the invention.
  • hydrates of the primary phosphates are similarly preferable.
  • colloidal silica in a proportion of 0.5 to 10 mol in terms of SiO 2 relative to PO 4 :1mol in the phosphates mentioned above.
  • the colloidal silica forms a low thermal expansion glass with the phosphates mentioned above to produce tension induced by a coating, and thus is an essential component.
  • the proportion be 0.5 mol or more and 10 mol or less in terms of SiO 2 relative to PO 4 :1 mol in the phosphates mentioned above.
  • the type of colloidal silica is not limited insofar as the stability of the solution or the compatibility with the phosphates mentioned above or the like is obtained.
  • ST-0 manufactured by Nissan Chemical Industries, LTD., SiO 2 content: 20 mass%, which is a commercially available acid-type, is mentioned, and an alkaline-type colloidal silica can also be used.
  • colloidal silica containing a sol containing aluminum (Al) can also be used.
  • the Al amount is preferably 1.0 or lower relative to Al 2 O 3 /SiO 2 ratio.
  • the treatment solution for insulation coating of the invention contains one or two or more members selected from permanganates of Mg, Sr, Zn, Ba, and Ca, which are divalent metals. It is also particularly important to adjust the content of the permanganates of divalent metals mentioned above to be in the range of 0.02 to 2.5 mol in total of Mg, Sr, Zn, Ba, and Ca relative to PO 4 :1 mol in the phosphates mentioned above.
  • the permanganates are contained in such a manner that the total amount of Mg, Sr, Zn, Ba, and Ca is 0.02 mol or more relative to PO 4 :1 mol in the phosphates.
  • the permanganates are contained in such a manner that the total amount of Mg, Sr, Zn, Ba, and Ca exceeds 2.5 mol, the thermal expansion of a coating increases to reduce the tension induced by a coating.
  • the total amount of Mg, Sr, Zn, Ba, and Ca is in the range of 0.2 to 1.0 mol.
  • the permanganates of the invention are compounds (metal salts) of (MnO 4 ) - and Mg, Sr, Zn, Ba, or Ca and may be hydrates thereof.
  • magnesium permanganate and strontium permanganate or hydrates thereof are preferable.
  • the reason for the increase in the moisture-absorption resistance due to the presence of at least one member selected from the permanganates of Mg, Sr, Zn, Ba, and Ca is considered as follows.
  • the colloidal silica and the phosphates form glass during baking treatment.
  • PO 4 in a free state in the phosphate that was not incorporated into the glass combines with the divalent metals of Mg, Sr, Zn, Ba, and Ca in the permanganates or Mn in the permanganates to form a compound insoluble in water in the insulation coating to thereby increase the moisture-absorption resistance.
  • Mg 3 (PO 4 ) 2 is considered to form in the insulation coating.
  • the permanganates uniformly dissolve in a coating under formation in baking treatment. Therefore, it is considered that PO 4 in a free state easily combines with Mg, Sr, Zn, Ba, Ca, or Mn to form a substance insoluble in water. This also contributes to the improvement of moisture-absorption resistance.
  • the concentration of the primary components mentioned above in the treatment solution for insulation coating there is no need of limiting the concentration of the primary components mentioned above in the treatment solution for insulation coating.
  • the concentration when the concentration is low, the insulation coating becomes thin.
  • the concentration is high, the viscosity of the treatment solution for insulation coating becomes high, resulting in the reduction in workability, such as application.
  • the concentration of colloidal silica and the permanganates of divalent metals mentioned above are naturally determined when the concentration of the phosphates are determined.
  • boric acid may be added.
  • one or two or more members selected from SiO 2 , Al 2 O 3 , and TiO 2 having a primary particle diameter of 50 to 2000 nm may be incorporated in the treatment solution for insulation coating of the invention.
  • the reason for requiring the sticking resistance is as follows.
  • a grain oriented electrical steel sheet is used for a wound core type transformer, the steel sheet is rolled to be formed into an iron core, and then subjected to strain relief annealing (e.g., about 800°C ⁇ about 3 hours). In that case, sticking between adjacent coatings sometimes arises. Such sticking reduces the insulation resistance between adjacent sheets of the iron core to thereby deteriorate the magnetic properties.
  • the content of the boric acid, SiO 2 , and the like and other additives be about 30 mass% or lower in total.
  • the treatment solution for insulation coating be chromium-free and is particularly preferable that the treatment solution for insulation coating does not substantially contain Cr.
  • “not substantially contain” means that Cr derived from impurities contained in the raw materials is permitted but Cr is not positively added.
  • components such as the phosphates, colloidal silica, and permanganates mentioned above, are available as commercially available items for industrial use in many cases. An amount of Cr as contained in these commercially available compounds as impurity is acceptable.
  • a steel slab for grain oriented electrical steel sheet having a given component composition is rolled to achieve a final sheet thickness. Thereafter, primary recrystallization annealing and secondary recrystallization annealing are performed, the treatment solution for insulation coating of the invention described above is applied to the steel sheet surface, and, subsequently the steel sheet is baked at a temperature of 350 to 1100°C.
  • the slab for grain oriented electrical steel sheet is subjected to hot rolling, then subjected to normalizing annealing as required, and then subjected to cold rolling once, or twice or more including intermediate annealing, to thereby achieve the final sheet thickness.
  • the component composition of the slab is not limited, and any known component composition is accepted.
  • the production method is also not limited, and any known production method can be used.
  • the primary components of a typical slab for grain oriented electrical steel sheet contain c: 0.10 mass% or lower, Si: 2.0 to 5.0 mass%, and Mn: 0.01 to 1.0 mass%. Si: 2.0 to 4.5 mass% is preferable.
  • various inhibitors are usually used, and elements according to the inhibitors are added in addition to the primary components mentioned above. For example, as the inhibitors,
  • the sheet thickness after hot rolling is preferably adjusted to be in the range of 1.5 to 3.0 mm.
  • the hot-rolled sheet after hot rolling may be subjected to normalizing annealing depending on requirement of a further improvement of magnetic properties and the like.
  • the hot-rolled sheet subjected to hot rolling or further normalizing annealing is subjected to cold rolling to achieve a final sheet thickness.
  • the cold rolling may be once, or the cold rolling may be twice or more including intermediate annealing performed between cold rollings.
  • the primary recrystallization annealing subsequent to the cold rolling is performed in order to accelerate the primary recrystallization, but may be performed together with decarburization by controlling the atmosphere or the like.
  • the treatment conditions of the primary recrystallization annealing can be set according to the purpose or the like, and continuous annealing is preferably performed at a temperature of 800 to 950°C for 10 to 600 seconds.
  • nitriding treatment can also be performed using ammonia gas or the like.
  • a subsequent secondary recrystallization annealing is a process for preferential growth of a so-called Goss orientation, i.e., the crystal orientation in which the magnetic properties are excellent in the rolling direction, by the secondary recrystallization, out of crystal grains obtained by the primary recrystallization annealing (primary recrystallized grain).
  • Goss orientation i.e., the crystal orientation in which the magnetic properties are excellent in the rolling direction
  • the conditions of the secondary recrystallization annealing can be set according to the purpose or the like.
  • the secondary recrystallization annealing is preferably performed at a temperature of 800 to 1250°C for about 5 to 300 hours.
  • an annealing separator containing MgO as a primary component i.e., sufficiently containing MgO
  • an annealing separator containing MgO as a primary component i.e., sufficiently containing MgO
  • the treatment solution for insulation treatment coating of the invention can be applied irrespective of the presence of the forsterite coating.
  • the treatment solution for insulation coating of the invention is applied to the grain oriented electrical steel sheet after the secondary recrystallization manufactured through a series of the processes described above, and then the steel sheet is baked.
  • the treatment solution for insulation coating may be diluted by adding water or the like to adjust the density for improvement of application properties.
  • known measures such as a roll coater, can be used.
  • the baking temperature is preferably 750°C or higher. This is because the tension induced by a coating arises by baking at 750°C or higher.
  • the baking temperature may be 350°C or higher. This is because, in the production of the iron core, strain relief annealing is performed at a temperature of about 800°C for about 3 hours in many cases, and in this case, the tension induced by a coating develops during the strain relief annealing.
  • the temperature is adjusted to be 1100°C or lower.
  • the maximum range of the baking temperature is 350°C or more and 1100°C or lower.
  • the thickness of the insulation coating is not limited and the thickness per one side is preferably in the range of 1 to 5 ⁇ m.
  • the tension induced by a coating is proportional to the thickness of the coating.
  • the thickness thereof is lower than 1 ⁇ m, the tension induced by a coating may be insufficient depending on purposes.
  • the thickness thereof exceeds 5 ⁇ m the lamination factor sometimes decreases more than necessary.
  • the thickness of the insulation coating can be adjusted to a target value by the concentration, the application amount, the application conditions (e.g., pressing conditions of a roll coater), etc., of the treatment solution for insulation coating.
  • a slab for grain oriented electrical steel sheet containing C: 0.05 mass%, Si: 3 mass%, sol.Al: 0.02 mass%, Mn: 0.04 mass%, S: 0.02 mass%, and a balance of Fe and inevitable impurities was hot-rolled to form a hot-rolled sheet having a sheet thickness of 2.0 mm, and then the hot-rolled sheet was subjected to normalizing annealing at 1000°C for 60 seconds. Thereafter, the hot-rolled sheet was subjected to a first cold rolling to have an intermediate sheet thickness of 1.5 mm, then subjected to intermediate annealing at 1100°C for 60 seconds, and then subjected to a second cold rolling to form a cold-rolled sheet having a final sheet thickness of 0.22 mm.
  • the cold-rolled sheet was subjected to primary recrystallization annealing at 820°C for 150 seconds with decarburization. Thereafter, an MgO slurry was applied thereto as an annealing separator, and then secondary recrystallization annealing was performed at 1200°C for 15 hours, thereby obtaining grain oriented electrical steel sheets having a forsterite coating.
  • treatment solutions for insulation coating in which 700 ml (containing 3 mol in terms of SiO 2 ) of colloidal silica (water base) and permanganates indicated in Table 1 in a proportion of 0.01 to 3.0 mol in total in terms of Mg, Sr, Zn, Ba, and Ca was incorporated in 500 ml of aqueous solution containing 1 mol of magnesium phosphate Mg(H 2 PO 4 ) 2 in terms of PO 4 were prepared.
  • As the amount of the treatment solution sufficient amount required for the following experiments was prepared while maintaining the mixing ratio mentioned above. The same applies below.
  • the treatment solutions for insulation coating were applied to the surface of the grain oriented electrical steel sheets, and the steel sheets were baked at 830°C for 1 minute. The thickness of the coating was adjusted so that the thickness per one side was 2 ⁇ m.
  • the grain oriented electrical steel sheets having an insulation coating thus obtained were evaluated for the tension induced by a coating, moisture-absorption resistance, rust resistance, and lamination factor by the following methods.
  • Test pieces having a width of 30 mm and a length of 280 mm were extracted by shearing from the grain oriented electrical steel sheet having an insulation coating while defining the lengthwise direction as the rolling direction, and, subsequently, the insulation coating on one of the both faces was removed.
  • the dimension of the amount of curvature deformation of one end of the test pieces was measured while fixing one end having a length of 30 mm in the lengthwise direction of the steel sheet, and the tension induced by a coating ⁇ was calculated from Equation (1).
  • the amount of curvature deformation was measured in such a manner that the lengthwise direction of the steel sheet was set to the horizontal direction and the width direction was set to the vertical direction, respectively.
  • test pieces 50 mm ⁇ 50 mm were extracted from the grain oriented electrical steel sheets having an insulation coating, and dipped and boiled for 5 minutes in 100°C distilled water. Then, the amount of elution of P of the coating surface was quantitatively analyzed, and the average value was determined to be used as the index of the moisture-absorption resistance.
  • the steel sheets having an insulation coating were held in the air having a temperature of 50°C and a dew point of 50°C for 50 hours, and then the steel sheet surface was visually observed, and evaluated based on the area ratio of portions where rust formed.
  • the lamination factor was evaluated by a method based on JIS C 2550.
  • insulation coatings that are all excellent in the coating properties of the tension induced by a coating, moisture-absorption resistance, rust resistance, and lamination factor were formed.
  • the insulation coating properties of the examples of the invention were equal to or more than those of the Comparative Examples to which chromium compounds were added.
  • a slab for grain oriented electrical steel sheet containing C: 0.03 mass%, Si: 3 mass%, sol.Al: lower than 0.01 mass%, Mn: 0.04 mass%, S: lower than 0.01 mass%, Se: 0.02 mass%, Sb: 0.03 mass%, and a balance of Fe and inevitable impurities was hot-rolled to form a hot-rolled sheet having a sheet thickness of 2.5 mm, and then the hot-rolled sheet was subjected to normalizing annealing at 1050°C for 60 seconds. Then, the hot-rolled sheet was subjected to a first cold rolling to form a cold-rolled sheet having an intermediate sheet thickness of 0.8 mm, and then subjected to intermediate annealing at 1000°C for 30 seconds.
  • the cold-rolled sheet was subjected to a second cold rolling to achieve a final sheet thickness of 0.30 mm.
  • the cold-rolled sheet having such a final sheet thickness was subjected to primary recrystallization annealing at 850°C for 60 seconds. Thereafter, an MgO slurry was applied thereto as an annealing separator, and then secondary recrystallization annealing was performed at 880°C for 50 hours, thereby obtaining grain oriented electrical steel sheets having a forsterite coating.
  • treatment solutions for insulation coating in which colloidal silica in a proportion of 0.5 to 10 mol (1000 ml of aqueous solution) in terms of SiO 2 and permanganates (0.5 mol in total of magnesium permanganate ⁇ hexahydrate [Mg(MnO 4 ) 2 ⁇ 6H 2 0] in a proportion of 0.2 mol in terms of Mg and zinc permanganate ⁇ hexahydrate [Zn(MnO 4 ) 2 ⁇ 6H 2 O] in a proportion of 0.3 mol in terms of Zn) were incorporated in 500 ml of aqueous solution of various phosphates indicated in Table 2 (containing 1 mol in terms of PO 4 ) were prepared. Then, the treatment solutions were applied to the surface of the grain oriented electrical steel sheets, and the steel sheets were baked at 800°C for 60 seconds. The coating thickness after the baking treatment was adjusted so that the thickness per one side was 3 ⁇ m.
  • the grain oriented electrical steel sheets after the baking treatment were evaluated for the tension induced by a coating, moisture-absorption resistance, rust resistance, and lamination factor by the same methods as in Example 1.
  • a slab for grain oriented electrical steel sheet containing C: 0.05 mass%, Si: 3 mass%, sol.Al: lower than 0.02 mass%, Mn: 0.04 mass%, S: 0.02 mass%, and a balance of Fe and inevitable impurities was hot-rolled to form a hot-rolled sheet having a sheet thickness of 2.0 mm, and then the hot-rolled sheet was subjected to normalizing annealing at 1000°C for 60 seconds. Then, the hot-rolled sheet was subjected to a first cold rolling to form a cold-rolled sheet having an intermediate sheet thickness of 1.5 mm, and then subjected to intermediate annealing at 1100°C for 60 seconds.
  • the cold-rolled sheet was subjected to a second cold rolling to achieve a final sheet thickness of 0.22 mm.
  • the cold-rolled sheet having such a final sheet thickness was subjected to primary recrystallization annealing at 820°C for 150 seconds with decarburization. Thereafter, an MgO slurry was applied thereto as an annealing separator, and then secondary recrystallization annealing was performed at 1200°C for 15 hours, thereby obtaining grain oriented electrical steel sheets having a forsterite coating.
  • Treatment solutions for insulation coating in which 700 ml (3 mol in terms of SiO 2 ) of colloidal silica and 0.5 mol of magnesium permanganate ⁇ hexahydrate [Mg(MnO 4 ) 2 ⁇ 6H 2 O] in terms of Mg were incorporated in the phosphate aqueous solution were prepared. Subsequently, the treatment solutions were applied to the surface of the grain oriented electrical steel sheets, and the steel sheets were baked for 30 seconds at temperatures (soaking temperature) indicated in Table 3. The coating thickness after the baking treatment was adjusted so that the thickness per one side was 1.5 ⁇ m.
  • the grain oriented electrical steel sheets after the baking treatment were evaluated for the tension induced by a coating, moisture-absorption resistance, rust resistance, and lamination factor by the same methods as in Example 1.
  • the tension induced by a coating was also evaluated after strain relief annealing at 800°C for 3 hours.
  • an insulation coating that are all excellent in the tension induced by a coating, moisture-absorption resistance, rust resistance, and lamination factor can be formed on the surface of a grain oriented electrical steel sheet, and thus the reduction in the magnetostriction of the grain oriented electrical steel sheet and further, the reduction in noise pollution can be achieved.
  • the use of the treatment solution for insulation coating of the invention allows production of a grain oriented electrical steel sheet having an insulation coating outstanding coating properties, which are equivalent to those obtained when treatment solutions for insulation coating containing chromium compounds are used, without generating waste liquid containing harmful chromium compounds.

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EP08792758.8A 2007-08-23 2008-08-20 Liquide de traitement de film isolant pour une tôle d'acier électromagnétique à grains orientés, et procédé pour produire une tôle d'acier électromagnétique à grains orientés avec un film isolant Active EP2182091B1 (fr)

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PCT/JP2008/065232 WO2009025389A1 (fr) 2007-08-23 2008-08-20 Liquide de traitement de film isolant pour une tôle d'acier électromagnétique à grains orientés, et procédé pour produire une tôle d'acier électromagnétique à grains orientés avec un film isolant

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US20160060465A1 (en) * 2013-05-10 2016-03-03 Henkel Ag & Co. Kgaa Chromium-Free Coating for the Electrical Insulation of Grain-Oriented Electrical Steel Strip
US10597539B2 (en) 2013-05-10 2020-03-24 Henkel Ag & Co. Kgaa Chromium-free coating for the electrical insulation of grain-oriented electrical steel strip
EP3135793A1 (fr) * 2014-04-24 2017-03-01 JFE Steel Corporation Liquide de traitement permettant la formation d'un film de revêtement isolant exempt de chrome sur une tôle d'acier électromagnétique à grains orientés et tôle d'acier électromagnétique à grains orientés revêtue d'un film isolant exempt de chrome
EP3135793A4 (fr) * 2014-04-24 2017-05-03 JFE Steel Corporation Liquide de traitement permettant la formation d'un film de revêtement isolant exempt de chrome sur une tôle d'acier électromagnétique à grains orientés et tôle d'acier électromagnétique à grains orientés revêtue d'un film isolant exempt de chrome
EP3266896A4 (fr) * 2015-03-05 2018-01-10 JFE Steel Corporation Tôle d'acier électromagnétique orientée et procédé de fabrication associé
US10889880B2 (en) 2015-03-05 2021-01-12 Jfe Steel Corporation Grain-oriented electrical steel sheet and method for manufacturing same
EP3508614A4 (fr) * 2016-08-30 2019-09-25 JFE Steel Corporation Métal revêtu, liquide de traitement pour formation de revêtement et procédé de production de métal revêtu
US11280003B2 (en) 2016-08-30 2022-03-22 Jfe Steel Corporation Coated metal, coating-forming treatment solution, and method for producing coated metal
US11692272B2 (en) 2016-08-30 2023-07-04 Jfe Steel Corporation Coated metal, coating-forming treatment solution, and method for producing coated metal
EP3913091A4 (fr) * 2019-01-16 2022-10-12 Nippon Steel Corporation Procédé de fabrication d'une tôle d'acier électrique à grains orientés

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JP2009052060A (ja) 2009-03-12
EP2182091A4 (fr) 2015-10-21
WO2009025389A1 (fr) 2009-02-26
JP5194641B2 (ja) 2013-05-08
CN101784698A (zh) 2010-07-21
KR101169236B1 (ko) 2012-08-02
EP2182091B1 (fr) 2018-10-10
CN101784698B (zh) 2011-09-21
RU2431697C1 (ru) 2011-10-20
KR20100046209A (ko) 2010-05-06
US20110067786A1 (en) 2011-03-24
US8535455B2 (en) 2013-09-17

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